Canonical Allele Identifier: PA2827107867
Gene: CNPPD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3146648
ClinVar RCV Id: RCV004442018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308320.2:p.Ala236Val
CA2117701
NM_001321391.2:c.707C>T